Jobs at Cellares

Lead and execute stabilization, scaling, and continuous improvement of GMP-critical systems (ERP, MES, QMS, PLM, LIMS, integrations). Act as a hands-on player-coach bridging Manufacturing, Quality, Supply Chain, Engineering, and Finance to ensure data integrity, traceability, audit readiness, and operational execution while governing releases, validations, vendor performance, and cross-system issue resolution.

The Automation Engineer will develop and optimize lab automation systems, validate QC workflows, and ensure functionality of automated systems for cell therapy manufacturing.

The Director, Operations Finance will oversee FP&A for the Operations organization, driving financial insights, cost forecasts, and operational efficiencies across manufacturing sites globally.

The Director, Corporate FP&A leads financial planning processes, collaborates with functional leaders, and provides analysis to drive financial performance in a biotechnology setting.

The Quality Control Analyst will perform analytical testing, including in-process, lot release, and stability testing while ensuring compliance with cGMP guidelines. They will also investigate discrepancies and support equipment validation and documentation for regulatory submissions.

The Senior Electrical Engineer will lead electrical design for automation equipment, ensuring compliance and managing design documentation. Responsibilities include collaborating with teams, conduct prototyping, and driving design reviews based on industry standards.

The Director of Enterprise Programs leads client programs in process development, managing teams, overseeing tech transfer, ensuring compliance, and optimizing manufacturing processes for cell therapies.

The Automation Equipment Engineer will monitor, troubleshoot, and enhance automation equipment, collaborating with teams to resolve issues and improve production systems.

The Senior Director, Supply Chain leads and develops the Supply Chain organization, implementing strategies for efficiency in materials management, logistics, and production planning within a biotech environment.

Lead system requirements, architecture, modeling, and verification for a cell therapy manufacturing platform. Support subsystem teams, perform system characterization, root-cause analysis, and drive design convergence and continuous improvement from R&D toward scale-up.

This role involves supporting cell therapy manufacturing processes, leading technology transfers, developing automation, ensuring GMP compliance, and collaborating across departments.

The Principal Enterprise Data Architect will design and operationalize a data platform, integrating various systems while leading data governance and AI readiness efforts.

Lead MSAT process knowledge, technology transfers, and process automation for cell therapy manufacturing. Drive GMP readiness, process validation, CAPA/FMEA, documentation, root-cause investigations, capacity modeling, and cross-functional stakeholder coordination to scale and improve manufacturing operations.

The position leads method transfer, validation, and optimization of cell therapy analytical methods while collaborating across departments to ensure compliance and support product development.

The Director of Quality Compliance will lead compliance activities, manage quality systems, ensure GMP adherence, and oversee inspections and audits.

The HR Business Partner serves as the on-site HR resource, providing employee support and managing HR processes in a manufacturing environment while partnering with leadership to ensure compliance and improve HR practices.

Lead a QC team at a GMP cell therapy manufacturing site to manage analytical testing, method development/validation, stability programs, equipment qualification, investigations (OOS), data review, regulatory documentation, and QC quality systems. Interface cross-functionally, support audits, train analysts, manage contract lab transfers, and assist regulatory dossier preparation.

Support MSAT technology transfer and scale-up for cell therapy manufacturing. Drive process automation, ensure GMP readiness, maintain process knowledge and capability through data analysis, lead root cause investigations, CAPA, change control, FMEA, and validation activities. Write SOPs and batch records, define equipment requirements, provide training, and coordinate cross-functional stakeholders.

The Manufacturing Supervisor oversees cGMP operations and manages the production of cell therapy products, ensuring compliance, team development, and process optimization.

The Manufacturing Support Services Specialist supports manufacturing and warehouse operations, performing routine procedures in a GMP environment, training new associates, and ensuring compliance with SOPs and safety policies.